Cancer Genetic Test / Oncogenomics Test
Know Your Risk Beforehand, Prevent Early, and Plan Your Health Accurately
Do you have “cancer risk genes” hidden within you?
Many people believe that “cancer is a disease that happens randomly,” without clear causes.
However, in reality, many types of cancer arise from mutations in genes, which may be inherited or caused by everyday behaviors.
What is Cancer Genetic Test / Oncogenomics Test?
Cancer Genetic Test or Oncogenomics Test is the analysis of individual genetic information to determine what type of cancer you might be at risk for. It also helps you plan your health, prevent early, or choose an appropriate treatment method if abnormalities are found early.
Examples of genes tested include:
- BRCA1 / BRCA2 (Breast and Ovarian Cancer)
- MLH1 / MSH2 (Colon Cancer)
- TP53, APC, ATM, and other genes related to various cancers
The test results help doctors accurately assess your risk level and create a more personalized health monitoring plan.
How is the Test Done?
At LINNA Clinic, the Cancer Genetic / Oncogenomics Test is done using convenient, safe, and highly accurate methods:
- Consult with a doctor to analyze your personal risk and family history.
- Blood draw to collect DNA samples.
- Analyze with Next Generation Sequencing (NGS) technology.
- Interpret results by expert medical professionals and receive personalized health advice.
Preparation Before the Test
- No need to fast or avoid food and drink before the test.
- Get adequate rest the night before.
- If you have a family history of cancer, be sure to inform the doctor in detail.
- Do not take the test if you are currently ill
Why Get Tested?
- To detect genetic mutations directly related to cancer.
- To assess future cancer risks, such as breast, ovarian, colon, lung cancer, etc.
- To use the information for planning screening, prevention, or monitoring health appropriately.
- For those already diagnosed with cancer, use the results to choose targeted treatments.
- Provide advice to direct family members if there are inherited genetic abnormalities.
Who Should Get Tested?
- Those with close family members who have cancer (especially breast, ovarian, colon, lung cancer).
- Individuals who want to know their risk in advance and plan for their health.
- People already diagnosed with cancer who need to select the best treatment based on genetic information.
- Women who are concerned about breast and ovarian cancer.
- Men with a family history of prostate cancer or colon cancer.
- Those planning to have children and want to assess hereditary genetic risks.
Summary
Cancer Genetic Test / Oncogenomics Test is a test to identify genetic cancer risks. It helps you understand which types of cancer your body might develop and allows you to plan for prevention or care early.
For those with a family history of cancer or those planning long-term health care, this test is an essential step in truly understanding your body.
At LINNA Clinic, we provide expert consultations and genetic testing with accurate and safe technology, ensuring you have the information you need to take care of yourself and your loved ones.
📍 To schedule your Cancer Genetic / Oncogenomics Test:
📲 Line: @linnaclinic
📞 Phone: 063-609-8888
📱 WhatsApp: +66 91 979 9554
Find and Order Laboratory Tests
Anti-Desmoglein 1 (Dsg1) Ab:
2,860 THB
Detects antibodies to desmoglein 1, used to diagnose pemphigus foliaceus, an autoimmune skin disease causing skin blistering.
serum 1-2 ml.
Autoimmune Panel,Skin Disorder Testing
11151
Specific IgE for Gluten(f79):
2,600 THB
Measures specific IgE antibodies to gluten, used to diagnose gluten sensitivity or wheat allergies.
serum 1 ml
Celiac Disease Panel,Food Allergy Testing
11152
FoundationOne Liquid (ACT) (FOUNDATION MEDICINE, INC.):
293,930 THB
Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
Whole blood in FoundationOne Liquid collection tubes (Streck BCT tube X 2) 1. ( Streck tube ) 2. + Request+Consent form Load Salesforce 3.
Cancer Genomic Panel,Liquid Biopsy Testing
11148
Pregnenolone, LC/MS/MS [Questdiagnostic]:
32,220 THB
Measures pregnenolone hormone levels, used to assess adrenal function and hormonal balance.
Serum 2 ml (DO NOT USE GEL TUBES)
Hormonal Panel,Adrenal Function Tests
11149
ANORA Miscarriage testing(BCC):
51,200 THB
Detects chromosomal abnormalities, large deletions or duplications, and uniparental disomy in miscarriage tissue to determine causes of pregnancy loss.
0.5 mm^3 tissue in container with NSS and maternal blood in Special kit **Fresh tissue in NSS and maternal EDTA blood 4-6 ml are alter- native in case of no anora kit** // PBS/NSS NSS BCC 17/11/22
Genetic Miscarriage Panel,Chromosomal Abnormality Testing
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FoundationOne HEME (Longitudinal Program case):
214,760 THB
Next-generation sequencing test for hematologic cancers (leukemia, sarcoma), identifying genomic alterations, including base substitutions, insertions, deletions, and rearrangements.
Turnaround Time 1 month
11145
Gene Agnostic Parallel (GTP) (Gene Agnostic):
212,459 THB
Gene-agnostic parallel sequencing test to identify genetic mutations associated with cancer.
1. Blood in streck tube (there are 2 streck tubes) and 2. FFPE tissue in collection kits
Hereditary Cancer Panel,Genetic Screening
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Screening for common drug(Urine):
10,238 THB
Screens for common drugs of abuse using liquid chromatography/tandem mass spectrometry (LC-MS/MS), with detection limits varying by substance.
random urine 50 ml (minimum 5 ml)
Toxicology Panel,Drug Abuse Testing
11147
Ethylbenzene (Sum of mandelic acid and phenyl- glyoxylic acid )(HPLC):
1,620 THB
Measures levels of ethylbenzene metabolites (mandelic acid and phenylglyoxylic acid) in urine, used to assess occupational exposure.
Random Urine 10-20 mL (End of Shift)
Occupational Health Panel,Toxicology Testing
11142
JAK2 V617F mutation:
7,088 THB
Detects JAK2 V617F mutation, associated with myeloproliferative disorders like polycythemia vera, using allele-specific PCR (AS-PCR).
EDTA whole blood 3-5 ml or EDTA bone marrow 3-5 ml
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Anti-Desmoglein 1 (Dsg1) Ab:
2,860 THB
Description: Detects antibodies to desmoglein 1, used to diagnose pemphigus foliaceus, an autoimmune skin disease causing skin blistering.
Specimen: serum 1-2 ml.
Related Tests: Autoimmune Panel,Skin Disorder Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Specific IgE for Gluten(f79):
2,600 THB
Description: Measures specific IgE antibodies to gluten, used to diagnose gluten sensitivity or wheat allergies.
Specimen: serum 1 ml
Related Tests: Celiac Disease Panel,Food Allergy Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
FoundationOne Liquid (ACT) (FOUNDATION MEDICINE, INC.):
293,930 THB
Description: Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
Specimen: Whole blood in FoundationOne Liquid collection tubes (Streck BCT tube X 2) 1. ( Streck tube ) 2. + Request+Consent form Load Salesforce 3.
Related Tests: Cancer Genomic Panel,Liquid Biopsy Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Pregnenolone, LC/MS/MS [Questdiagnostic]:
32,220 THB
Description: Measures pregnenolone hormone levels, used to assess adrenal function and hormonal balance.
Specimen: Serum 2 ml (DO NOT USE GEL TUBES)
Related Tests: Hormonal Panel,Adrenal Function Tests
Add to WishlistRemove from Wishlist
Add to Wishlist
ANORA Miscarriage testing(BCC):
51,200 THB
Description: Detects chromosomal abnormalities, large deletions or duplications, and uniparental disomy in miscarriage tissue to determine causes of pregnancy loss.
Specimen: 0.5 mm^3 tissue in container with NSS and maternal blood in Special kit **Fresh tissue in NSS and maternal EDTA blood 4-6 ml are alter- native in case of no anora kit** // PBS/NSS NSS BCC 17/11/22
Related Tests: Genetic Miscarriage Panel,Chromosomal Abnormality Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
FoundationOne HEME (Longitudinal Program case):
214,760 THB
Description: Next-generation sequencing test for hematologic cancers (leukemia, sarcoma), identifying genomic alterations, including base substitutions, insertions, deletions, and rearrangements.
Specimen: Turnaround Time 1 month
Add to WishlistRemove from Wishlist
Add to Wishlist
Gene Agnostic Parallel (GTP) (Gene Agnostic):
212,459 THB
Description: Gene-agnostic parallel sequencing test to identify genetic mutations associated with cancer.
Specimen: 1. Blood in streck tube (there are 2 streck tubes) and 2. FFPE tissue in collection kits
Related Tests: Hereditary Cancer Panel,Genetic Screening
Add to WishlistRemove from Wishlist
Add to Wishlist
Screening for common drug(Urine):
10,238 THB
Description: Screens for common drugs of abuse using liquid chromatography/tandem mass spectrometry (LC-MS/MS), with detection limits varying by substance.
Specimen: random urine 50 ml (minimum 5 ml)
Related Tests: Toxicology Panel,Drug Abuse Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Ethylbenzene (Sum of mandelic acid and phenyl- glyoxylic acid )(HPLC):
1,620 THB
Description: Measures levels of ethylbenzene metabolites (mandelic acid and phenylglyoxylic acid) in urine, used to assess occupational exposure.
Specimen: Random Urine 10-20 mL (End of Shift)
Related Tests: Occupational Health Panel,Toxicology Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
JAK2 V617F mutation:
7,088 THB
Description: Detects JAK2 V617F mutation, associated with myeloproliferative disorders like polycythemia vera, using allele-specific PCR (AS-PCR).
Specimen: EDTA whole blood 3-5 ml or EDTA bone marrow 3-5 ml
Related Tests: Myeloproliferative Disease Panel,JAK2 Testing
Add to WishlistRemove from Wishlist
Add to Wishlist